(Q36481170)

14 August 2017

Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families (English)

1 reference

14 August 2017

M Reiff

1

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author name string

K Ross

2

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14 August 2017

S Mulchandani

3

1 reference

14 August 2017

K J Propert

4

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14 August 2017

R E Pyeritz

5

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14 August 2017

N B Spinner

6

1 reference

14 August 2017

B A Bernhardt

7

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14 August 2017

18 September 2012

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14 August 2017

1 reference

14 August 2017

83

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14 August 2017

1

1 reference

14 August 2017

23-30

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To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts.

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Exploring concordance and discordance for return of incidental findings from clinical sequencing

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

"What does it mean?": uncertainties in understanding results of chromosomal microarray testing

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Varieties of uncertainty in health care: a conceptual taxonomy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Copy number and SNP arrays in clinical diagnostics

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Why is genetic screening for autosomal dominant disorders underused in families? The case of hereditary hemorrhagic telangiectasia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

The clinical context of copy number variation in the human genome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Chromosomal microarray interpretation: what is a child neurologist to do?

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Genetic testing: considerations for pediatric nephrologists

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Whole genome scanning: resolving clinical diagnosis and management amidst complex data

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Motivating factors for physician ordering of factor V Leiden genetic tests

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Understanding incidental findings in the context of genetics and genomics

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Differential use of available genetic tests among primary care physicians in the United States: results of a national survey

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Educational needs in genetic medicine: primary care perspectives

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Genetic testing and breach of patient confidentiality: law, ethics, and pragmatics

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Communicating genetic information: a difficult challenge for future pediatricians

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

The incidentalome: a threat to genomic medicine

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Clinical genetic evaluation of the child with mental retardation or developmental delays

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Ethical issues raised by genetic testing with oligonucleotide microarrays

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Genetic testing: psychological aspects and implications

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Ethical issues with genetic testing in pediatrics

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Ethical issues in genetic testing of children

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Psychological impact of genetic testing for adult-onset disorders. An update for clinicians.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

What is a meaningful result? Disclosing the results of genomic research in autism to research participants

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Identification of incestuous parental relationships by SNP-based DNA microarrays.

28 June 2018

1 reference

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.

21 January 2018

1 reference

Whole-genome sequencing and the physician.

21 January 2018

1 reference

From genetics to genomics: ethics, policy, and parental decision-making

21 January 2018

1 reference

What keeps you up at night? Genetics professionals' distressing experiences in patient care.

21 January 2018

1 reference

The evolving duty to disclose the presence of genetic disease to relatives

21 January 2018

1 reference

Family communication matters: the impact of telling relatives about unclassified variants and uninformative DNA-test results.

21 January 2018

1 reference

Beyond information: exploring patients' preferences.

21 January 2018

1 reference

Genomics education for health care professionals in the 21st century.

21 January 2018

1 reference

A blueprint for maternal and child health primary care physician education in medical genetics and genomic medicine: recommendations of the United States secretary for health and human services advisory committee on heritable disorders in newborns a

21 January 2018

1 reference

An ethical imperative: genetics education for physicians and patients.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Generic Consent for Genetic Screening

21 October 2018

1 reference

Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527693

Molecular technologies open new clinical genetic vistas

21 October 2018

1 reference

12 December 2020

The coming explosion in genetic testing--is there a duty to recontact?

1 reference

12 December 2020

Incidence and predictors of positive and negative effects of BRCA1/2 genetic testing on familial relationships: a 3-year follow-up study

1 reference

12 December 2020

Empowering primary care health professionals in medical genetics: how soon? How fast? How far?

1 reference

12 December 2020

ASHG statement. Professional disclosure of familial genetic information. The American Society of Human Genetics Social Issues Subcommittee on Familial Disclosure

1 reference

12 December 2020

Identifiers

DOI

10.1111/CGE.12004

1 reference

14 August 2017

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14 August 2017

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